WO2004015032A1

WO2004015032A1 - Process for hydrogenation of aromatics in hydrocarbon feedstocks containing thiopheneic compounds

Info

Publication number: WO2004015032A1
Application number: PCT/US2003/024924
Authority: WO
Inventors: Paul Benjeman Himelfarb; Charles Eugene Wilson
Original assignee: Shell Internationale Research Maatschappij B.V.
Priority date: 2002-08-07
Filing date: 2003-08-06
Publication date: 2004-02-19
Also published as: US7081555B2; BR0313313A; KR100980137B1; US20040030208A1; EP1546289B1; NO20050602L; PT1546289E; CN1678718A; JP2006500434A; EP1546289A1; IN2005DE00420A; UA78844C2; US20060167327A1; AR040789A1; ATE332953T1; RU2005106232A; JP4436757B2; US7230148B2; KR20050056955A; DE60306789D1

Abstract

The present invention relates to an improved process for the hydrogenation of aromatics in hydrocarbon feedstocks containing thiopheneic compounds as impurities, the aromatics hydrogenation being conducted in a hydrogenation reactor in the presence of a nickel based catalyst. The improvement comprises operating the hydrogenation reactor at a reaction temperature sufficiently high from the start of a run, that the thiopheneic compounds are decomposed and substantially absorbed into the bulk of the nickel catalyst, thereby substantially extending the life of the catalyst.

Description

PROCESS FOR HYDROGENATION OF AROMATICS IN HYDROCARBON FEEDSTOCKS CONTAINING THIOPHENEIC COMPOUNDS

Field of the Invention

The present invention is directed to a process for the hydrogenation of aromatics using nickel based catalysts. More particularly, the present invention relates to the hydrogenation of aromatics in hydrocarbon feedstocks containing thiopheneic compounds, which are known to deactivate nickel catalysts and to substantially reduce catalyst life.

Background of the Invention

Nickel-containing catalysts are widely used to hydrogenate aromatic compounds in various hydrocarbon feedstocks. Because of the sensitivity of nickel catalysts to poisoning by sulfur compounds commonly found in such feedstocks, the feedstocks are normally desulfurized to a considerable degree prior to being contacted with the nickel catalyst. Despite the desulfurization step, it is not uncommon for small amounts of sulfur impurities to remain in the feedstocks, including aromatic sulfur compounds, such as thiophene, benzothiophene and dibenzothiophene, which are particularly poisonous to supported nickel catalysts.

Because the poisoning of nickel catalysts by sulfur compounds is a severe world- wide problem, extensive studies have been conducted in various laboratories in an attempt to determine the mechanism of sulfur poisoning, sometimes with conflicting results. For example, in the work by Poels, E.K., van Beek, W. P., den Hoed, W., Nisser, C. (1995); Fuel Vol. 74 No. 12, pp 1800-1805, sulfur poisoning on a variety of nickel catalysts having a wide range of nickel surface area was evaluated. The authors concluded for all the catalysts tested that surface poisoning by sulfur was the predominate deactivation mechanism. This study suggested that sulfur absorption could be switched from surface to bulk using higher temperature and lower sulfur content in the feeds.

However, they concluded that moving into bulk sulfur absorption did not extend catalyst life, as a surface layer still controlled catalyst deactivation. Others have reported that bulk sulfur absorption can occur with thiol type sulfur, but not with thiophenes. While there may be disagreement as to the precise mechanism of sulfur poisoning, it is generally accepted that the toxicity of sulfur compounds found in hydrocarbon feedstocks increases with the molecular weight and the complexity of the molecule, with thiopheneic compounds, such as thiophene, benzothiophene and dibenzothiophene being especially detrimental to nickel catalysts. A possible explanation for this is that higher molecular weight sulfur compounds, such as thiopheneic compounds, are not as readily decomposed ^• as thiols, sulfϊdes and mercaptans, but instead are adsorbed on the surface of the nickel catalyst forming a stable surface species which blocks active catalyst sites. This adsorption of thiopheneic compounds on the surface of the catalyst is generally believed, to be irreversible due to the high heat of adsorption of these compounds. Since surface adsorption of sulfur compounds reduces active sites, catalyst vendors often quote catalyst lifetimes based on the sulfur in the feed and flows to get roughly one layer coverage of sulfur on the surface of the catalyst. Nickel based catalysts used to hydrogenate aromatics in feedstocks containing thiopheneic compounds generally have shorter catalyst lives than feedstocks containing lower molecular weight sulfur compounds, because of the tendency of the thiopheneic compounds under conventional process conditions to be adsorbed on the surface of the catalyst, thereby deactivating it. Accordingly, it can be seen that an aromatics hydrogenation process operated in such a manner that thiopheneic compounds in the feedstock did not poison or deactivate the nickel based catalyst employed in the process, would be highly desirable. The present invention provides such an improved process.

Summary of the Invention

It has now been found, contrary to teachings in the prior art, that the lifetimes of nickel based catalysts exposed to thiopheneic compounds present in hydrocarbon feedstocks can be extended for considerable periods of time by control of certain process conditions as hereinafter described. Accordingly, the present invention is directed to an improved process for the hydrogenation of aromatics in hydrocarbon feedstocks containing thiopheneic compounds as impurities, the aromatics hydrogenation being conducted in a hydrogenation reactor in the presence of nickel based catalysts. The improvement comprises operating the hydrogenation reactor at a reaction temperature sufficiently high from the start of a run, that the thiopheneic compounds are decomposed and substantially absorbed into the bulk of the nickel based catalyst. It has been found that by operating the reactor at a higher reaction temperature from the start of the run, the thiopheneic compounds decompose and enter into the bulk nickel, instead of being adsorbed on the surface of the catalyst, thereby decreasing the poisoning impact of the thiopheneic compounds and substantially extending the life of the catalyst.

Brief Description of the Drawings Figure 1 is a graph showing the effect of reaction temperature on sulfur poisoning of a nickel catalyst by a thiopheneic compound in a hydrocarbon solvent feedstock. The results are expressed in terms of as aromatics concentration in the product as a function of sulfur exposure and reaction temperature.

Figure 2 is a graph showing aromatics concentration in the product from the hydrogenation of a hydrocarbon solvent feedstock containing different thiopheneic compounds at different concentrations.

Figure 3 is a graph showing the attempted recovery of a deactivated nickel catalyst by raising the temperature to elevated levels.

Detailed Description of the Invention

The present invention relates to an improved process for hydrogenating aromatics in hydrocarbon feedstocks containing thiopheneic compounds using nickel based catalysts. The term "thiopheneic compounds" as used herein.is intended to include relatively high molecular weight aromatic sulfur compounds such as thiophene, benzothiophene, dibenzothiophene and the like, which are known poisons to nickel based catalysts.

The improved aromatics hydrogenation process of the present invention involves contacting a hydrocarbon feedstock containing aromatics and thiopheneic compounds with an activated nickel based catalyst in a reactor, at a relatively high reaction temperature from the, start of the run. Typically, a new charge of nickel catalyst is "activated" following a procedure recommended by the catalyst vendor. The activation procedure usually involves heating the catalyst in the reactor at specified heating rates and for specified periods of time in flowing hydrogen which reduces the nickel catalyst thereby activating it. Specifically, this step reduces nickel oxide to nickel metal. The latter is the active site in the catalyst. After the catalyst is "activated" the reactor is cooled down and the run is started by introducing hydrocarbon feedstock into the reactor with hydrogen. Because, nickel catalysts are generally believed to deactivate more rapidly at higher temperatures, commercial aromatics hydrogenation reactors are normally started at the lowest temperature required to meet product specifications. As the catalyst deactivates over time, the reactor temperature is raised to compensate for the loss in activity.

The basis for the present invention is the surprising discovery that by operating the aromatics hydrogenation process at an elevated temperature from the start of the run, it is possible to convert thiopheneic compounds into species that are diffused or absorbed into the bulk of the nickel catalyst instead of forming surface species which poison the catalyst. Because of this, nickel catalysts employed in the improved process of the invention have longer lifetimes, in some cases up to three times or more the lifetimes of catalysts run on the same feed at a lower starting temperature. A further surprising discovery is that if the process is operated at a lower temperature initially and the catalyst deactivates, the activity cannot be restored by raising the temperature to elevated levels thereafter. It appears that once the thiopheneic compounds are adsorbed on the surface of the catalyst and cover a substantial number of active sites, it is difficult to substantially restore lost activity. Thus, the key to the improved process of the present invention is to operate the process at an elevated temperature from the start of the run, and to maintain the process at a temperature sufficiently high that the thiopheneic compounds present in the feedstock continue to be converted into a species which is absorbed into the catalyst bulk, instead of being adsorbed on the catalyst surface. The term "start of the run" as used herein generally refers to the point in time that feedstock containing thiopheneic compounds and hydrogen are first introduced into a reactor containing a new or fresh charge of active nickel based catalyst. "Start of the run" generally does not include any catalyst activation procedure per se, which is normally accomplished in the absence of feedstock. While it is preferred to bring the reactor to the required high temperature from the time feedstock and hydrogen are first introduced into the reactor, the term "start of the run" in its broader sense is intended to include any point in time before the nickel catalyst adsorbs a substantial amount of thiopheneic compounds on its surface. Thus, short delays in bringing the reactor to the required temperature after feedstock introduction is still considered to come within meaning of "start of the run", and to be within the scope of the present invention.

The term "reaction temperature" refers to the temperature at which the hydrocarbon feedstock and hydrogen make initial contact with active nickel catalyst in the reactor. In a typical fixed-bed downflow reactor with a fresh charge of catalyst, the "reaction temperature" will be essentially the same as the reactor inlet temperature. Since the hydrogenation of aromatics is an exothermic reaction, there will usually be temperature differential across the catalyst bed, with the reactor outlet temperature normally being higher than the reactor inlet temperature. As a run progresses, that portion of catalyst in the reactor with the greatest exposure to sulfur compounds will deactivate first, and hydrogenation of aromatics will occur in subsequent portions of the catalyst bed until there is insufficient active catalyst remaining in order to meet product specifications, at which time the catalyst will be need to be replaced.

In practice of the improved process of the present invention it is critical that the reaction temperature be maintained from the start of the run sufficiently high that the thiopheneic compounds present in the hydrocarbon feedstock will be converted to into a species which is absorbed in the bulk of the nickel, instead of being adsorbed on the surface of the catalyst. It is also important that the temperature throughout the reactor not exceed the temperature at which unwanted side reactions, such as cracking will occur. While the reaction temperature in accordance with the present invention may vary somewhat depending on the activity of the nickel based catalyst being used and the particular reactor design, the reaction temperature from the start of the run will generally range from about 140°C to about 225°C, preferably from about 149°C to about 200°C, and most preferably from 150°C to about 175°C. Based on the foregoing teachings and the examples, it will be apparent to those skilled in the art what reaction temperatures to employ to obtain bulk sulfiding of thiopheneic compounds in various other types of reactors which may be used for aromatics hydrogenation.

Other suitable process conditions for carrying out the improved aromatics hydrogenation process of the invention include a total pressure of about 200 psig to about 800 psig, preferably from about 300 psig to about 600 psig, and a liquid hourly space velocity (LHSN) of from about 0.5 to about 5.0, preferably from about 1.0 to about 3.0.

Hydrogen use in terms of hydrogen consumption basis the total hydrogen flow is in the range of from about 5% to about 80%, preferably in the range of from about 20% to about 50%. Hydrocarbon feedstocks suitable for use in the improved aromatics hydrogenation process of the present invention include any hydrocarbon or mixture of hydrocarbons boiling in the range of about 80°C to about 350°C and containing from about 1 w% to about 80 w% aromatics, up to 100 w% aromatics, preferably from about 2 w% to about 50 w% aromatics. It is noted that in commercial practice with higher aromatic concentrations in the feed, it is typical to dilute the feed with product recycle to control heat release, thereby diluting the actual aromatic level reaching the catalyst in the reactor.

The improved aromatics hydrogenation process of the invention can be employed to reduce the aromatics concentration in the hydrocarbon feedstocks being treated to the desired level. For example, depending on product specifications, to levels of less than about 0.2 w%, less than about 0.02 w%, or even less than about 0.002 w%, (the latter value being the limit of detection).

Suitable feedstocks include light and heavy solvents, white oils, naphtha, kerosene, diesel and the like containing from 0.1 ppm to 50 ppm thiopheneic compounds, preferably from about 0.2 ppm to about 10 ppm thiopheneic compounds. The improved process of the invention is particularly advantageous in the dearomatization of hydrocarbon solvent feedstocks, such as light and heavy solvents, including naphtha, boiling in the range of ^' from about 80°C to about 350°C. Applications for the solvent products after hydrogenation include use in coatings (paint, varnishes and lacquers), industrial cleaners, printing inks, extractive processes, and pharmaceuticals.

Any modern nickel based catalyst may be employed in the improved aromatics hydrogenation process of the invention. This includes catalysts prepared by impregnation referred as supported nickel catalysts and also those prepared by coprecipitation referred to as bulk nickel catalysts. Supported nickel catalysts which may be used in the process of the invention will generally have a nickel content of from about 10 w% to about 35 w%, preferably from about 15 w% to about 30 w%. Bulk nickel catalysts which may be used in the process of the invention will generally have a nickel content from about 20 w% to about 80 w%, with a nickel content of about 30 w% to about 70 w% being preferred. The nickel contents are all based on final, activated (reduced) catalyst. Thus, the overall range of nickel contents for the nickel based catalysts suitable for use in the improved process of the invention is from about 10 w% to about 80 w%. The nickel catalysts suitable for use in the present process may include minor amounts of other catalytic metals as long as such metals do not interfere with the decomposition of the thiopheneic compounds and formation of the bulk sulfur species.

Suitable supports for supported nickel based catalysts include one or more refractory oxides such as alumina, silica, silica alumina, titania, zirconia and combinations thereof. Alumina, silica, or mixtures thereof, are particularly preferred supports. The BET surface area of the final catalyst may range from about 40 m² /g to about 300 m² /g, preferably from about 80 m² /g to about 250 m² /g.

The following examples will serve to illustrate the invention disclosed herein. These examples are intended only as a means of illustration and should not be construed as limiting the scope of the invention in any way. Those skilled in the art will recognize many variations that may be made without departing from the spirit of the disclosed invention.

Example 1 : A set of experiments was conducted to demonstrate the effect of reaction temperature on the poisoning of supported nickel catalysts used for hydrogenation of hydrocarbon feedstocks containing thiopheneic compounds. The catalyst used in these experiments was a commercially available high activity nickel catalyst containing 28 w% nickel on an alumina support having a BET surface area of 120-140 m² /g. The catalyst was supplied in a pre-reduced and air stabilized form. A 25 cc portion of the catalyst

(with a 1:6 dilution with silicon carbide to ensure catalyst particle wetting) was placed in a conventional fixed-bed down-flow reactor. The catalyst was activated in flowing hydrogen at approximately 8 liters/hour by heating the catalyst to 120°C at 40°C/hr and holding for two hours, followed by heating to 230°C at 40°C/hr and holding for an additional two hours to reduce surface nickel oxide. The catalyst was then cooled to room temperature.

Five runs were conducted using a hydrocarbon solvent feedstock with a boiling point range of from 103°C to 302°C, with an aromatics content of 17 w%, and containing approximately 50 ppm of benzothiophene. Each of the five runs was conducted at process conditions including: a LHSN of 1, a pressure of 530 psig, volume hydrogen/volume feed of approximately 500. The only variable between the different runs was the reaction temperature. For Run 1 the reaction temperature from the start of the run was 52°C. For Run 2 the reaction temperature from the start of the run was 93°C. For Run 3 the reaction temperature from the start of the run was 121 °C. For each of Runs 4 and 5 the reaction temperature from the start of the runs was 149°C.

The results of these five runs, showing aromatics concentration as a function of sulfur exposure (i.e., benzothiophene exposure) and reaction temperature, is presented in Figure 1. Note that the sulfur exposure, given as a percent of sulfur per weight of catalyst, is calculated bases the sulfur (benzothiophene) level in the feed passed over the catalyst. At the lowest temperature (52°C), the catalyst almost immediately deactivates with negligible sulfur (0.1 w%) on the catalyst. At moderate temperatures (92°C and 121 °C), the catalyst appears deactivated at about 2 w% sulfur on the catalyst. At the higher reaction temperature of 149°C, which is in accordance with the present invention, there is no indication of catalyst deactivation with over 6 w% sulfur on the catalyst. The catalyst used in Run 5 was analyzed for sulfur content and was found to have 6.5 w%, which is in good agreement with the calculated value. The sulfur level in the product was measured periodically in Runs 4 and 5 and was always less than 1 ppm, while the feed had about 50 ppm. Thus, all the benzothiophene in the feed passed over the catalyst was converted to a species which was absorbed on/into the catalyst bulk without deactivating it.

The foregoing experiments indicate that at low temperatures (52°C) deactivation occurs very rapidly, partially due to low activity of the catalyst at this temperature, with sulfur loading increasing the deactivation rate. At moderate temperatures (93 °C and 121°C)₅ the catalyst showed a rapid deactivation at about 2% sulfur loading, which level corresponds to approximately one monolayer coverage over the available nickel surface. At the higher reaction temperature (149°C), in accordance with the invention, the sulfur level of 6.5 w% on the catalyst when the run was stopped corresponds to over three monolayers coverage, which together with the continued high activity, indicates bulk sulfiding is occurring instead of deactivating surface sulfiding.

Example 2:

To demonstrate that the bulk nickel sulfiding observed with benzothiophene at high temperatures was applicable to other thiopheneic compounds, a further study was conducted using thiophene, as well as benzothiophene at two different concentration levels. This study involved two additional runs (Runs 6 and 7) using the same catalyst, hydrocarbon solvent feedstock and process conditions as in Example 1, except all the runs were conducted at a temperature of 149°C. The only variables between the three runs was the concentration and type of thiopheneic compounds which were as follows: Run 6 approximately 50 ppm thiophene, Run 5 approximately 50 ppm benzothiophene (same as in Example 1, above), and Run 7 approximately 400 ppm benzothiophene. The results of these three runs are shown in Figure 2. The results of Runs 5 and 6 show that thiophene behaves similar to benzothiophene and that bulk sulfiding can be obtained for either, provided the proper reaction temperature is employed from the start of the run. In Run 7 the catalyst was deactivated with approximately 3.5 % sulfur loading, as compared to no apparent deactivation with sulfur loadings up to 6.5 % for Runs 5 and 6. This indicates that at very high concentrations of thiopheneic compounds in the feedstock (400 ppm), the surface sulfur poisoning has a greater effect on the catalyst and can reduce the beneficial effects of bulk sulfiding.

Example 3

An experiment was conducted to determine if the activity of a catalyst poisoned by sulfur adsorbed on the surface of the catalyst at low or moderate reaction temperatures, could be recovered by raising the reaction temperature to a higher temperature were bulk sulfiding takes place. In this experiment, after the catalyst in Run 2 at 93 °C was surface sulfur poisoned, the reaction temperature was raised in several steps to 200°C. From the results of this experiment shown in Figure 3, it can be seen that by raising the temperature further deactivation can be stopped, but the activity already lost can be only marginally recovered, in spite of the fact that the upper temperature used (200°C) was over 50°C higher than required for bulk sulfur deposition had the proper reaction temperature been used from the start of the run.

The above examples demonstrate that sulfur poisoning by thiopheneic compounds of supported nickel catalysts used for aromatics hydrogenation can be avoided in accordance with the improved process of the present invention, by employing a reaction temperature from the start of the run which is conducive to the absorption of the sulfur into the bulk of the nickel, rather than being adsorbed on the surface of the catalyst. Because more than three times as much sulfur from thiopheneic compounds can be absorbed into the bulk of the catalyst without deactivating it, the improved process of the present invention results in a dramatic enhancement of catalyst life, e.g., up to a threefold or more increase.

Claims

We Claim:

I . In a process for the hydrogenation of aromatics in a hydrocarbon feedstock also containing thiopheneic compounds as impurities, said aromatics hydrogenation being ^• conducted in a hydrogenation reactor in the presence of a nickel based catalyst, the improvement which comprises operating said hydrogenation reactor at a reaction temperature sufficiently high from the start of a run that said thiopheneic compounds are decomposed and substantially absorbed into the bulk of said nickel based catalyst, thereby extending the life of said nickel based catalyst.

2. The process of claim 1 wherein the aromatics in the hydrocarbon feedstock comprise from about 1 w% to about 100 w% aromatics.

3. The process of claim 1 wherein the hydrocarbon feedstock contains from about 0.1 ppm to about 50 ppm thiopheneic compounds.

4. The process of claim 3 wherein the thiopheneic compounds comprise thiophene, benzothiophene, dibenzothiophene and mixtures thereof.

5. The process of claim 1 wherein said nickel based catalyst contains from about 10 w% to about 80 w% nickel.

6. The process of claim 5 wherein said nickel based catalyst is a supported nickel catalyst and contains from about 10 w% to about 35 w% nickel.

7. The process of claim 5 wherein said nickel based catalyst is a bulk nickel catalyst and contains from about 20 w% to about 80 w% nickel.

8. The process on claim 6 wherein the support for said supported nickel catalyst is alumina, silica or mixtures thereof.

9. The process of claim 1 wherein the hydrocarbon feedstock is a hydrocarbon solvent feedstock having a boiling point range of from about 80°C to about 350°C

10. The process of claim 9 wherein the aromatics in the hydrocarbon feedstock comprise from about 2 w% to about 50 w% aromatics.

I I . The process of claim 1 wherein the aromatics content of the product after hydrogenation is less than about 0.2 w%.

12. The process of claim 1 wherein said nickel based catalyst has a surface area of from about 40 m /g to about 300 m²/g.

13. The process of claim 1 wherein the reaction temperature is maintained below the temperature where any substantial cracking occurs.

14. The process of claim 10 wherein the hydrocarbon feedstock contains from about 0.2 ppm to about 10 ppm thiopheneic compounds.

15. The process of claim 6 wherein said supported nickel catalyst contains from about 15 w% to about 30 w% nickel.

16. The process of claim 15 wherein said supported nickel catalyst has a surface area of from about 80 m²/g to about 250 m²/g.

17. The process of claim 1 wherein the reaction temperature from the start of the run is in the range of from about 140°C to about 225°C.

18. The process of claim 17 wherein the total pressure is from about 200 psig to about 800 psig

19. The process of claim 18 wherein the LHSN is from about 0.5 to about 5.0.

20. The process of claim 19 wherein the hydrogen consumption basis the total hydrogen flow is from about 5% to about 80%.

21. The process of claim 5 wherein the reaction temperature from the start of the run is in the range of from about 149°C to about 200°C.

22. The process of claim 21 wherein the total pressure is from about 300 psig to about 600 psig.

23. The process of claim 22 wherein the LHSN is from about 1.0 to about 3.0.

24. The process of claim 23 wherein the hydrogen consumption basis the total hydrogen flow is from about 20% to about 50%.

25. The process of claim 5 wherein said supported nickel catalyst has a surface area of from about 80 m² /g to about 250 m² /g.

26. The process of claim 16 wherein the reaction temperature from the start of the run is in the range of from about 150°C to about 175°C.

27. The process of claim 1 wherein the lifetime of said nickel based catalyst is extended threefold or more as compared to the same catalyst started at a reaction temperature below which said thiopheneic compounds are absorbed into the bulk of said nickel based catalyst.

28. The process of claim 26 wherein the lifetime of said supported nickel catalyst is extended threefold or more as compared to the same catalyst started at a reaction temperature below which said thiopheneic compounds are absorbed into the bulk of said supported nickel catalyst